Claritin Reditabs (loratadine) NDC 11523-7202

NDC codes

FDA NDC Directory

Product NDC (as listed)11523-7202Labeler and product segments. Claims need a package NDC.

Product NDC at billing width11523-7202Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
11523-7202-1	11523720201	3 BLISTER PACK in 1 CARTON (11523-7202-1) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Dec 12, 2006
11523-7202-3	11523720203	1 BLISTER PACK in 1 CARTON (11523-7202-3) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACKMarketed from Dec 12, 2006

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Claritin ReditabsSuffix: Reditabs
Generic name (nonproprietary): loratadine
Active ingredients: Loratadine — 5 mg/1
Dosage form: Tablet, Orally disintegrating
Route: Oral
Labeler: Bayer HealthCare LLC
Product type: Over-the-counter drug
Marketing category: NDA — New Drug ApplicationApplication NDA 021993
Marketing start: Dec 12, 2006
Listing expires: Dec 31, 2026
Identifiers: Product ID 11523-7202_45371bc6-b83d-a96d-e063-6294a90a7c40SPL ID 45371bc6-b83d-a96d-e063-6294a90a7c40SPL set ID 7dc04b48-f053-4e4b-a493-9e8286d2a791RxCUI 672558, 904026UNII 7AJO3BO7QN

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N411523720201 followed by a unit qualifier and the quantity

Package 11523-7202-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Dec 5, 2025.

Indications (excerpt from the label)

Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose itchy, watery eyes sneezing itching of the nose or throat

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)